• Welcome to Phoenix Rising!

    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

    To become a member, simply click the Register button at the top right.

Search results

  1. C

    Has anyone with ME (irrespective of COVID status) been on PAXLOVID?

    Before I begin I want to apologize for the poor formatting. I am typing this on my phone and I expect the formatting will be less than optimal. I know this thread is a few months old at this point but I wanted to add my experience here. I was diagnosed with ME/CFS in 2015 and have had...
  2. C

    Doctors in Wilington, NC

    I am actually a patient at Hunter Hopkins. They are not in network for my insurance, so I have to pay out of pocket. It is not cheap but I certainly feel like it will be worth it in the long run. I sat and talked with the doctor for longer than I have ever talked with a doctor before. I think...